Variant #0000278829 (NC_000010.10:g.88441279G>T, NC_000010.10(NM_001080114.1):c.321+1365G>T (LDB3))
Chromosome |
10 |
Allele |
Unknown |
Affects function (as reported) |
Does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.88441279G>T |
DNA change (hg38) |
g.86681522G>T |
Published as |
LDB3(NM_001171610.2):c.408G>T (p.P136=) |
ISCN |
- |
DB-ID |
LDB3_000130 |
Variant remarks |
VKGL data sharing initiative Nederland |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
CLASSIFICATION record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0 View details |
Owner |
VKGL-NL_AMC |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_AMC |
Date created |
2018-01-15 20:58:59 +01:00 (CET) |
Date last edited |
2020-06-28 14:22:01 +02:00 (CEST) |

Variant on transcripts
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